{ "source": "curated_targets.json", "sha256": "21e807af380b71a62b0172f519415ed9130ca46986b6cd5543418dac950c1839", "snapshot_date": "2026-10-11", "count": 381, "section": "demostracion", "verified_count": 0, "recipe": 7, "unavailable_count": 13, "record_fields": [ "pdb", "name", "family", "organism", "resolution", "chain" ], "records": [ [ "1AJ6", "NOVOBIOCIN-RESISTANT MUTANT (R136H) OF THE N-TERMINAL 24 KDA FRAGMENT", "topoisomerase", "ESCHERICHIA COLI", 2.3, "A" ], [ "1BN1", "CA2 (Carbonic Anhydrase II)", "metalloenzyme", "Homo sapiens", 2.1, "A" ], [ "1C3P", "CRYSTAL STRUCTURE OF AN HDAC HOMOLOG FROM AQUIFEX AEOLICUS", "hydrolase", "AQUIFEX AEOLICUS", 1.8, "A" ], [ "1C3R", "CRYSTAL STRUCTURE OF AN HDAC HOMOLOG COMPLEXED WITH TRICHOSTATIN A", "hydrolase", "AQUIFEX AEOLICUS", 2, "A" ], [ "1C3S", "CRYSTAL STRUCTURE OF AN HDAC HOMOLOG COMPLEXED WITH SAHA", "hydrolase", "AQUIFEX AEOLICUS", 2.5, "A" ], [ "1C6X", "ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2.5, "A" ], [ "1CBR", "CRYSTAL STRUCTURE OF CELLULAR RETINOIC-ACID-BINDING PROTEINS I AND II", "nuclear_receptor", "MUS MUSCULUS", 2.9, "A" ], [ "1CBS", "CRYSTAL STRUCTURE OF CELLULAR RETINOIC-ACID-BINDING PROTEINS I AND II", "nuclear_receptor", "Homo sapiens", 1.8, "A" ], [ "1CX2", "CYCLOOXYGENASE-2 (PROSTAGLANDIN SYNTHASE-2) COMPLEXED WITH A SELECTIVE", "oxidoreductase", "MUS MUSCULUS", 3, "A" ], [ "1DIY", "CRYSTAL STRUCTURE OF ARACHIDONIC ACID BOUND IN THE CYCLOOXYGENASE", "oxidoreductase", "OVIS ARIES", 3, "A" ], [ "1EI1", "DIMERIZATION OF E. COLI DNA GYRASE B PROVIDES A STRUCTURAL MECHANISM", "topoisomerase", "ESCHERICHIA COLI", 2.3, "A" ], [ "1EPB", "STRUCTURE OF THE EPIDIDYMAL RETINOIC ACID-BINDING PROTEIN AT 2.1", "nuclear_receptor", "RATTUS NORVEGICUS", 2.2, "A" ], [ "1F0R", "CRYSTAL STRUCTURE OF HUMAN COAGULATION FACTOR XA COMPLEXED WITH RPR208815", "protease", "Homo sapiens", 2.1, "A" ], [ "1FE2", "CRYSTAL STRUCTURE OF DIHOMO-GAMMA-LINOLEIC ACID BOUND IN THE CYCLOOXYGENASE CHANNEL OF PROSTAGLANDIN ENDOPEROXIDE H SYNTHASE-1.", "oxidoreductase", "OVIS ARIES", 3, "A" ], [ "1FEM", "CRYSTALLOGRAPHIC STUDIES ON COMPLEXES BETWEEN RETINOIDS AND PLASMA", "nuclear_receptor", "BOS TAURUS", 1.9, "A" ], [ "1FH0", "CRYSTAL STRUCTURE OF HUMAN CATHEPSIN V COMPLEXED WITH AN IRREVERSIBLE", "protease", "Homo sapiens", 1.6, "A" ], [ "1GKU", "REVERSE GYRASE FROM ARCHAEOGLOBUS FULGIDUS", "topoisomerase", "ARCHAEOGLOBUS FULGIDUS", 2.7, "B" ], [ "1GPK", "Structure of Acetylcholinesterase Complex with (+)-Huperzine A at 2.1A Resolution", "hydrolase", "Torpedo californica", 2.1, "A" ], [ "1GX9", "BOVINE BETA-LACTOGLOBULIN COMPLEXED WITH RETINOIC ACID, TRIGONAL", "nuclear_receptor", "BOS TAURUS", 2.34, "A" ], [ "1HSG", "HIV-1 Protease", "protease", "Human immunodeficiency virus 1", 2, "A" ], [ "1HVY", "Human thymidylate synthase complexed with dUMP and Raltitrexed, an antifolate drug, is in the closed conformation", "methyltransferase", "Homo sapiens", 1.9, "A" ], [ "1HWK", "HMG-CoA Reductase", "oxidoreductase", "Homo sapiens", 2.22, "A" ], [ "1IAS", "CYTOPLASMIC DOMAIN OF UNPHOSPHORYLATED TYPE I TGF-BETA RECEPTOR", "growth_factor", "Homo sapiens", 2.9, "B" ], [ "1IGZ", "CRYSTAL STRUCTURE OF LINOLEIC ACID BOUND IN THE CYCLOOXYGENASE CHANNEL", "oxidoreductase", "OVIS ARIES", 2.9, "A" ], [ "1IRU", "Ubiquitina-Proteasoma Target (1IRU)", "proteasome", "BOS TAURUS", 2.75, "Q" ], [ "1IS0", "CRYSTAL STRUCTURE OF A COMPLEX OF THE SRC SH2 DOMAIN WITH", "kinase", "ROUS SARCOMA VIRUS", 1.9, "A" ], [ "1ITO", "CRYSTAL STRUCTURE ANALYSIS OF BOVINE SPLEEN CATHEPSIN B-E64C COMPLEX", "protease", "BOS TAURUS", 2.29, "A" ], [ "1J36", "CRYSTAL STRUCTURE OF DROSOPHILA ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.4, "A" ], [ "1J37", "CRYSTAL STRUCTURE OF DROSOPHILA ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.4, "A" ], [ "1J38", "CRYSTAL STRUCTURE OF DROSOPHILA ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.6, "A" ], [ "1KIJ", "CRYSTAL STRUCTURE OF THE 43K ATPASE DOMAIN OF THERMUS THERMOPHILUS", "topoisomerase", "THERMUS THERMOPHILUS", 2.3, "A" ], [ "1KLI", "Cofactor-and substrate-assisted activation of factor VIIa", "protease", "Homo sapiens", 1.69, "H" ], [ "1KTZ", "CRYSTAL STRUCTURE OF THE HUMAN TGF-BETA TYPE II RECEPTOR EXTRACELLULAR", "growth_factor", "Homo sapiens", 2.15, "A" ], [ "1KZN", "CRYSTAL STRUCTURE OF E. COLI 24KDA DOMAIN IN COMPLEX WITH CLOROBIOCIN", "topoisomerase", "ESCHERICHIA COLI", 2.3, "A" ], [ "1M17", "EGFR Kinase Domain", "kinase", "Homo sapiens", 2.6, "A" ], [ "1M6D", "CRYSTAL STRUCTURE OF HUMAN CATHEPSIN F", "protease", "Homo sapiens", 1.7, "A" ], [ "1M9Z", "CRYSTAL STRUCTURE OF HUMAN TGF-BETA TYPE II RECEPTOR LIGAND BINDING", "growth_factor", "Homo sapiens", 1.05, "A" ], [ "1NHY", "Crystal Structure of the GST-like Domain of Elongation Factor 1-gamma from Saccharomyces cerevisiae.", "transferase", "Saccharomyces cerevisiae", 3, "A" ], [ "1Q4G", "2.0 ANGSTROM CRYSTAL STRUCTURE OF OVINE PROSTAGLANDIN H2 SYNTHASE-1,", "oxidoreductase", "OVIS ARIES", 2, "A" ], [ "1RKP", "CRYSTAL STRUCTURE OF PDE5A1-IBMX", "phosphodiesterase", "Homo sapiens", 2.05, "A" ], [ "1RV7", "CRYSTAL STRUCTURES OF A MULTIDRUG-RESISTANT HIV-1 PROTEASE REVEAL AN", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2.7, "A" ], [ "1RYP", "Ubiquitina-Proteasoma Target (1RYP)", "proteasome", "SACCHAROMYCES CEREVISIAE", 1.9, "W" ], [ "1SM3", "CRYSTAL STRUCTURE OF THE TUMOR SPECIFIC ANTIBODY SM3 COMPLEX WITH ITS PEPTIDE EPITOPE", "protein_interaction", "MUS MUSCULUS", 1.95, "L" ], [ "1SO2", "CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B In COMPLEX WITH A DIHYDROPYRIDAZINE INHIBITOR", "phosphodiesterase", "Homo sapiens", 2.4, "A" ], [ "1SUU", "STRUCTURE OF DNA GYRASE A C-TERMINAL DOMAIN", "topoisomerase", "BORRELIA BURGDORFERI", 1.75, "A" ], [ "1T69", "CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH SAHA", "hydrolase", "Homo sapiens", 2.91, "A" ], [ "1TGJ", "HUMAN TRANSFORMING GROWTH FACTOR-BETA 3, CRYSTALLIZED FROM DIOXANE", "growth_factor", "Homo sapiens", 2, "A" ], [ "1UZJ", "INTEGRIN BINDING CBEGF22-TB4-CBEGF33 FRAGMENT OF HUMAN FIBRILLIN-1,", "protein_interaction", "Homo sapiens", 2.25, "A" ], [ "1VKG", "CRYSTAL STRUCTURE OF HUMAN HDAC8 COMPLEXED WITH CRA-19156", "hydrolase", "Homo sapiens", 2.2, "A" ], [ "1VL4", "CRYSTAL STRUCTURE OF A PUTATIVE MODULATOR OF A DNA GYRASE (TM0727)", "topoisomerase", "THERMOTOGA MARITIMA", 1.95, "B" ], [ "1VPB", "CRYSTAL STRUCTURE OF A PUTATIVE MODULATOR OF DNA GYRASE (BT3649) FROM", "topoisomerase", "BACTEROIDES THETAIOTAOMICRON", 1.75, "A" ], [ "1W22", "CRYSTAL STRUCTURE OF INHIBITED HUMAN HDAC8", "hydrolase", "Homo sapiens", 2.5, "A" ], [ "1WBK", "HIV-1 PROTEASE IN COMPLEX WITH ASYMMETRIC INHIBITOR, BEA568", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2, "A" ], [ "1WBM", "HIV-1 PROTEASE IN COMPLEX WITH SYMMETRIC INHIBITOR, BEA450", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2, "A" ], [ "1X7R", "CRYSTAL STRUCTURE OF ESTROGEN RECEPTOR ALPHA COMPLEXED WITH GENISTEIN", "nuclear_receptor", "Homo sapiens", 2, "A" ], [ "1XP0", "PDE5A (Phosphodiesterase-5)", "phosphodiesterase", "Homo sapiens", 1.79, "A" ], [ "1XWD", "CRYSTAL STRUCTURE OF HUMAN FOLLICLE STIMULATING HORMONE COMPLEXED WITH", "gpcr", "Homo sapiens", 2.92, "A" ], [ "1ZZ1", "CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH SAHA BOUND", "hydrolase", "ALCALIGENACEAE BACTERIUM", 1.57, "A" ], [ "2A3W", "DECAMERIC STRUCTURE OF HUMAN SERUM AMYLOID P-COMPONENT BOUND TO BIS-1,", "protein_interaction", "Homo sapiens", 2.2, "A" ], [ "2AM9", "Androgen Receptor LBD", "nuclear_receptor", "Homo sapiens", 1.64, "A" ], [ "2AW1", "CARBONIC ANHYDRASE INHIBITORS: VALDECOXIB BINDS TO A DIFFERENT ACTIVE", "metalloenzyme", "Homo sapiens", 1.46, "A" ], [ "2AYL", "2.0 Angstrom Crystal Structure of Manganese Protoporphyrin IX-reconstituted Ovine Prostaglandin H2 Synthase-1 Complexed With Flurbiprofen", "oxidoreductase", "OVIS ARIES", 2, "A" ], [ "2B2A", "CRYSTAL STRUCTURE OF THE TEN DOMAIN OF THE TELOMERASE REVERSE", "polymerase", "TETRAHYMENA THERMOPHILA", 2.22, "A" ], [ "2BQV", "HIV-1 PROTEASE IN COMPLEX WITH INHIBITOR AHA455", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2.1, "A" ], [ "2CEN", "P1' EXTENDED HIV-1 PROTEASE INHIBITORS ENCOMPASSING A TERTIARY ALCOHOL", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.7, "A" ], [ "2FR3", "CRYSTAL STRUCTURE OF CELLULAR RETINOIC ACID BINDING PROTEIN TYPE II IN", "nuclear_receptor", "Homo sapiens", 1.48, "A" ], [ "2GH6", "CRYSTAL STRUCTURE OF A HDAC-LIKE PROTEIN WITH 9,9,9-TRIFLUORO-8-OXO-N-", "hydrolase", "ALCALIGENACEAE BACTERIUM FB188", 2.2, "A" ], [ "2H02", "Structural studies of protein tyrosine phosphatase beta catalytic domain in complex with inhibitors", "hydrolase", "Homo sapiens", 2.3, "A" ], [ "2HZI", "ABL1 Kinase Imatinib", "kinase", "Homo sapiens", 1.7, "A" ], [ "2I3U", "Structural studies of protein tyrosine phosphatase beta catalytic domain in complex with inhibitors", "hydrolase", "Homo sapiens", 1.85, "A" ], [ "2I4G", "Structural studies of protein tyrosine phosphatase beta catalytic domain in complex with a sulfamic acid (soaking experiment)", "hydrolase", "Homo sapiens", 1.65, "A" ], [ "2I4H", "Structural studies of protein tyrosine phosphatase beta catalytic domain co-crystallized with a sulfamic acid inhibitor", "hydrolase", "Homo sapiens", 2.15, "A" ], [ "2J4O", "STRUCTURE OF TAB1", "protein_interaction", "Homo sapiens", 2.25, "A" ], [ "2JDI", "Ground state structure of F1-ATPase from bovine heart mitochondria (Bovine F1-ATPase crystallised in the absence of azide)", "atp_synthase", "Bos taurus", 1.9, "A" ], [ "2LBD", "LIGAND-BINDING DOMAIN OF THE HUMAN RETINOIC ACID RECEPTOR GAMMA BOUND", "nuclear_receptor", "Homo sapiens", 2.06, "A" ], [ "2NNJ", "CYP2C8dH complexed with felodipine", "cytochrome_p450", "Homo sapiens", 2.28, "A" ], [ "2OA8", "Crystal Structure of mTREX1 with ssDNA", "nuclease", "MUS MUSCULUS", 2.1, "A" ], [ "2OYE", "INDOMETHACIN-(R)-ALPHA-ETHYL-ETHANOLAMIDE BOUND TO CYCLOOXYGENASE-1", "oxidoreductase", "OVIS ARIES", 2.85, "P" ], [ "2OYU", "INDOMETHACIN-(S)-ALPHA-ETHYL-ETHANOLAMIDE BOUND TO CYCLOOXYGENASE-1", "oxidoreductase", "OVIS ARIES", 2.7, "P" ], [ "2P4E", "PCSK9 (Proprotein Convertase)", "protease", "Homo sapiens", 1.98, "A" ], [ "2QCQ", "CRYSTAL STRUCTURE OF BONE MORPHOGENETIC PROTEIN-3 (BMP-3)", "growth_factor", "Homo sapiens", 2.21, "A" ], [ "2R4G", "THE HIGH RESOLUTION STRUCTURE OF THE RNA-BINDING DOMAIN OF TELOMERASE", "polymerase", "TETRAHYMENA THERMOPHILA", 1.71, "A" ], [ "2VE3", "RETINOIC ACID BOUND CYANOBACTERIAL CYP120A1", "nuclear_receptor", "SYNECHOCYSTIS SP.", 2.1, "A" ], [ "2W96", "CDK4 (Apo/Cyclin D1)", "kinase", "Homo sapiens", 2.3, "B" ], [ "2X8Z", "CRYSTAL STRUCTURE OF ANCE-CAPTOPRIL COMPLEX", "protease", "DROSOPHILA MELANOGASTER", 1.98, "A" ], [ "2X90", "CRYSTAL STRUCTURE OF ANCE-ENALAPRILAT COMPLEX", "protease", "DROSOPHILA MELANOGASTER", 1.98, "A" ], [ "2XAB", "HSP90 Heat Shock Protein", "chaperone", "Homo sapiens", 1.9, "A" ], [ "2XWT", "CRYSTAL STRUCTURE OF THE TSH RECEPTOR IN COMPLEX WITH A BLOCKING TYPE", "gpcr", "Homo sapiens", 1.9, "A" ], [ "2ZHR", "CRYSTAL STRUCTURE OF BACE1 IN COMPLEX WITH OM99-2 AT PH 5.0", "protease", "Homo sapiens", 2.5, "A" ], [ "2ZJT", "CRYSTAL STRUCTURE OF DNA GYRASE B' DOMAIN SHEDS LIGHTS ON THE", "topoisomerase", "MYCOBACTERIUM TUBERCULOSIS", 2.8, "A" ], [ "3DU6", "STRUCTURE OF THE CATALYTIC SUBUNIT OF TELOMERASE, TERT", "polymerase", "TRIBOLIUM CASTANEUM", 2.71, "B" ], [ "3DY3", "Ubiquitina-Proteasoma (3DY3)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.81, "K" ], [ "3DY4", "Ubiquitina-Proteasoma (3DY4)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.8, "H" ], [ "3DZY", "Intact PPAR gamma - RXR alpha Nuclear Receptor Complex on DNA bound with Rosiglitazone, 9-cis Retinoic Acid and NCOA2 Peptide", "nuclear_receptor", "Homo sapiens", 3.1, "D" ], [ "3E50", "CRYSTAL STRUCTURE OF HUMAN INSULIN DEGRADING ENZYME IN COMPLEX WITH", "protease", "Homo sapiens", 2.3, "A" ], [ "3ERT", "ER Alpha (Estrogen Receptor)", "nuclear_receptor", "Homo sapiens", 1.9, "A" ], [ "3F75", "ACTIVATED TOXOPLASMA GONDII CATHEPSIN L (TGCPL) IN COMPLEX WITH ITS", "protease", "TOXOPLASMA GONDII", 1.99, "A" ], [ "3FHV", "STRUCTURAL BASIS OF SALMONELLA TYPHI TYPE IVB PILS AND CYSTIC FIBROSIS", "protein_interaction", "SALMONELLA TYPHI", 1.9, "A" ], [ "3FLI", "Discovery of XL335, a Highly Potent, Selective and Orally-Active Agonist of the Farnesoid X Receptor (FXR)", "nuclear_receptor", "Homo sapiens", 2, "A" ], [ "3G04", "CRYSTAL STRUCTURE OF THE TSH RECEPTOR IN COMPLEX WITH A THYROID-", "gpcr", "Homo sapiens", 2.55, "A" ], [ "3G0E", "KIT kinase domain in complex with sunitinib", "kinase", "Homo sapiens", 1.6, "A" ], [ "3G7E", "CRYSTAL STRUCTURE OF E. COLI GYRASE B CO-COMPLEXED WITH PROP-2-YN-1-YL", "topoisomerase", "ESCHERICHIA COLI", 2.2, "A" ], [ "3GEN", "The 1.6 A crystal structure of human bruton's tyrosine kinase bound to a pyrrolopyrimidine-containing compound", "kinase", "Homo sapiens", 1.6, "A" ], [ "3GPJ", "Ubiquitina-Proteasoma (3GPJ)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.7, "H" ], [ "3GPT", "Ubiquitina-Proteasoma (3GPT)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.41, "H" ], [ "3HH2", "CRYSTAL STRUCTURE OF THE MYOSTATIN:FOLLISTATIN 288 COMPLEX", "growth_factor", "MUS MUSCULUS", 2.15, "C" ], [ "3HYE", "Ubiquitina-Proteasoma (3HYE)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.5, "H" ], [ "3IG0", "CRYSTAL STRUCTURE OF THE SECOND PART OF THE MYCOBACTERIUM TUBERCULOSIS", "topoisomerase", "MYCOBACTERIUM TUBERCULOSIS", 2.1, "A" ], [ "3JTG", "CRYSTAL STRUCTURE OF MOUSE ELF3 C-TERMINAL DNA-BINDING DOMAIN IN", "transcription_factor", "MUS MUSCULUS", 2.2, "A" ], [ "3KD2", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF", "ion_channel", "PSEUDOMONAS AERUGINOSA UCBPP-PA14", 1.8, "A" ], [ "3KDA", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF WITH THE H269A", "ion_channel", "PSEUDOMONAS AERUGINOSA UCBPP-PA14", 1.5, "A" ], [ "3KJF", "Caspase 3 Bound to a covalent inhibitor", "protease", "Homo sapiens", 2, "A" ], [ "3KK6", "CRYSTAL STRUCTURE OF CYCLOOXYGENASE-1 IN COMPLEX WITH CELECOXIB", "oxidoreductase", "OVIS ARIES", 2.75, "A" ], [ "3KYL", "STRUCTURE OF THE CATALYTIC SUBUNIT OF TELOMERASE BOUND TO ITS RNA", "polymerase", "TRIBOLIUM CASTANEUM", 2.7, "A" ], [ "3L1B", "COMPLEX STRUCTURE OF FXR LIGAND-BINDING DOMAIN WITH A", "nuclear_receptor", "Homo sapiens", 1.9, "A" ], [ "3L54", "Structure of Pi3K gamma with inhibitor", "kinase", "Homo sapiens", 2.3, "A" ], [ "3LBD", "LIGAND-BINDING DOMAIN OF THE HUMAN RETINOIC ACID RECEPTOR GAMMA BOUND", "nuclear_receptor", "Homo sapiens", 2.4, "A" ], [ "3MG0", "Ubiquitina-Proteasoma (3MG0)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.68, "H" ], [ "3MXJ", "Crystal Structure of the mTREX1 Apoprotein", "nuclease", "MUS MUSCULUS", 1.95, "A" ], [ "3N8W", "CRYSTAL STRUCTURE OF R120Q/NATIVE CYCLOOXYGENASE-1 HETERODIMER MUTANT", "oxidoreductase", "OVIS ARIES", 2.75, "A" ], [ "3N8X", "CRYSTAL STRUCTURE OF CYCLOOXYGENASE-1 IN COMPLEX WITH NIMESULIDE", "oxidoreductase", "OVIS ARIES", 2.75, "A" ], [ "3N8Y", "STRUCTURE OF ASPIRIN ACETYLATED CYCLOOXYGENASE-1 IN COMPLEX WITH", "oxidoreductase", "OVIS ARIES", 2.6, "A" ], [ "3N8Z", "CRYSTAL STRUCTURE OF CYCLOOXYGENASE-1 IN COMPLEX WITH FLURBIPROFEN", "oxidoreductase", "OVIS ARIES", 2.9, "A" ], [ "3O96", "Crystal Structure of Human AKT1 with an Allosteric Inhibitor", "kinase", "Homo sapiens", 2.7, "A" ], [ "3OSK", "CTLA-4 Immune Checkpoint", "protein_interaction", "Homo sapiens", 1.8, "A" ], [ "3P88", "FXR BOUND TO ISOQUINOLINECARBOXYLIC ACID", "nuclear_receptor", "Homo sapiens", 2.95, "A" ], [ "3P89", "FXR BOUND TO A QUINOLINECARBOXYLIC ACID", "nuclear_receptor", "Homo sapiens", 2.3, "A" ], [ "3PP0", "Crystal Structure of the Kinase domain of Human HER2 (erbB2).", "kinase", "Homo sapiens", 2.25, "A" ], [ "3QXX", "Crystal structure of dethiobiotin synthetase (BioD) from Helicobacter pylori complexed with GDP and 8-aminocaprylic acid", "ligase", "Helicobacter pylori", 1.36, "A" ], [ "3RUT", "FXR WITH SRC1 AND GSK359", "kinase", "Homo sapiens", 3, "A" ], [ "3RUU", "FXR WITH SRC1 AND GSK237", "kinase", "Homo sapiens", 2.5, "A" ], [ "3RVY", "CRYSTAL STRUCTURE OF THE NAVAB VOLTAGE-GATED SODIUM CHANNEL", "ion_channel", "ARCOBACTER BUTZLERI", 2.7, "A" ], [ "3RVZ", "CRYSTAL STRUCTURE OF THE NAVAB VOLTAGE-GATED SODIUM CHANNEL", "ion_channel", "ARCOBACTER BUTZLERI", 2.8, "A" ], [ "3RW0", "CRYSTAL STRUCTURE OF THE NAVAB VOLTAGE-GATED SODIUM CHANNEL", "ion_channel", "ARCOBACTER BUTZLERI", 2.95, "A" ], [ "3S43", "HIV-1 PROTEASE TRIPLE MUTANTS V32I, I47V, V82I WITH ANTIVIRAL DRUG", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.26, "A" ], [ "3SRW", "S. aureus Dihydrofolate Reductase complexed with novel 7-aryl-2,4-diaminoquinazolines", "oxidoreductase", "Staphylococcus aureus", 1.7, "X" ], [ "3V94", "TCRPDEC1 CATALYTIC DOMAIN IN COMPLEX WITH INHIBITOR WYQ16", "phosphodiesterase", "TRYPANOSOMA CRUZI", 2.33, "A" ], [ "3WZE", "KDR in complex with ligand sorafenib", "kinase", "Homo sapiens", 1.9, "A" ], [ "4AF3", "Human Aurora B Kinase in complex with INCENP and VX-680", "kinase", "Homo sapiens", 2.75, "A" ], [ "4AUA", "Liganded X-ray crystal structure of cyclin dependent kinase 6 (CDK6)", "kinase", "Homo sapiens", 2.31, "A" ], [ "4AZY", "DESIGN AND SYNTHESIS OF BACE1 INHIBITORS WITH IN VIVO BRAIN REDUCTION", "protease", "Homo sapiens", 1.79, "A" ], [ "4BCF", "Structure of CDK9 in complex with cyclin T and a 2-amino-4-heteroaryl- pyrimidine inhibitor", "kinase", "Homo sapiens", 3.01, "A" ], [ "4BVN", "Ultra-thermostable beta1-adrenoceptor with cyanopindolol bound", "gpcr", "Meleagris gallopavo", 2.1, "A" ], [ "4CA7", "DROSOPHILA ANGIOTENSIN CONVERTING ENZYME (ANCE) IN COMPLEX WITH A", "protease", "DROSOPHILA MELANOGASTER", 1.82, "A" ], [ "4CA8", "DROSOPHILA ANGIOTENSIN CONVERTING ENZYME (ANCE) IN COMPLEX WITH A", "protease", "DROSOPHILA MELANOGASTER", 1.99, "A" ], [ "4CVL", "PaMurF in complex with AMP-PNP", "ligase", "Pseudomonas aeruginosa PAO1", 2.98, "A" ], [ "4DLN", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF WITH THE D129S", "ion_channel", "PSEUDOMONAS AERUGINOSA", 1.55, "A" ], [ "4DM7", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF WITH THE E153D", "ion_channel", "PSEUDOMONAS AERUGINOSA", 1.36, "A" ], [ "4DMF", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF WITH THE H177A", "ion_channel", "PSEUDOMONAS AERUGINOSA", 2.12, "B" ], [ "4DQC", "Crystal Structure of (G16C/L38C) HIV-1 Protease in Complex with DRV", "protease", "Human immunodeficiency virus 1", 1.94, "A" ], [ "4DUH", "CRYSTAL STRUCTURE OF 24 KDA DOMAIN OF E. COLI DNA GYRASE B IN COMPLEX", "topoisomerase", "ESCHERICHIA COLI", 1.5, "A" ], [ "4E4N", "JAK1 kinase (JH1 domain) in complex with compound 49", "kinase", "Homo sapiens", 1.9, "A" ], [ "4EJJ", "Human Cytochrome P450 2A6 in complex with nicotine", "cytochrome_p450", "Homo sapiens", 2.3, "A" ], [ "4EU2", "Ubiquitina-Proteasoma (4EU2)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.51, "H" ], [ "4FK3", "BRAF V600E Kinase", "kinase", "Homo sapiens", 2.65, "A" ], [ "4I04", "STRUCTURE OF ZYMOGEN OF CATHEPSIN B1 FROM SCHISTOSOMA MANSONI", "protease", "SCHISTOSOMA MANSONI", 1.95, "D" ], [ "4I5H", "Crystal Structure of a Double Mutant Rat Erk2 Complexed With a Type II Quinazoline Inhibitor", "kinase", "Rattus norvegicus", 1.9, "A" ], [ "4IAQ", "CRYSTAL STRUCTURE OF THE CHIMERIC PROTEIN OF 5-HT1B-BRIL IN COMPLEX", "gpcr", "HOMO SAPIENS, ESCHERICHIA COLI", 2.8, "A" ], [ "4IAR", "CRYSTAL STRUCTURE OF THE CHIMERIC PROTEIN OF 5-HT1B-BRIL IN COMPLEX", "gpcr", "HOMO SAPIENS, ESCHERICHIA COLI", 2.7, "A" ], [ "4JP9", "SPIROCYCLIC BETA-SITE AMYLOID PRECURSOR PROTEIN CLEAVING ENZYME 1", "protein_interaction", "Homo sapiens", 1.8, "A" ], [ "4JPC", "SPIROCYCLIC BETA-SITE AMYLOID PRECURSOR PROTEIN CLEAVING ENZYME 1", "protein_interaction", "Homo sapiens", 1.8, "A" ], [ "4JPE", "SPIROCYCLIC BETA-SITE AMYLOID PRECURSOR PROTEIN CLEAVING ENZYME 1", "protein_interaction", "Homo sapiens", 1.8, "A" ], [ "4JPS", "Co-crystal Structures of the Lipid Kinase PI3K alpha with Pan and Isoform Selective Inhibitors", "kinase", "Homo sapiens", 2.2, "A" ], [ "4JSX", "structure of mTORDeltaN-mLST8-Torin2 complex", "kinase", null, 3.5, "B" ], [ "4JV6", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX TO INHIBITOR-1", "phosphodiesterase", "Homo sapiens", 1.87, "B" ], [ "4JV8", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX WITH RAC-S1", "phosphodiesterase", "Homo sapiens", 1.45, "B" ], [ "4JVB", "CRYSTAL STRUCTURE OF PDE6D IN COMPLEX WITH THE INHIBITOR RAC-2", "phosphodiesterase", "Homo sapiens", 1.75, "B" ], [ "4JVF", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX WITH THE INHIBITOR (S)-5", "phosphodiesterase", "Homo sapiens", 2.4, "B" ], [ "4JYV", "Structure of factor VIIA in complex with the inhibitor (2R)-2-[3-ETHOXY-4-(PROPAN-2-YLOXY)PHENYL]-2-(ISOQUINOLIN-6-YLAMINO)-N-[(3-SULFAMOYLPHENYL)SULFONYL]ETHANAMIDE", "protease", "Homo sapiens", 2.19, "H" ], [ "4JZD", "Structure of factor VIIA in complex with the inhibitor 2-{2-[(4-carbamimidoylphenyl)carbamoyl]-6-methoxypyridin-3-yl}-5-{[(2S)-1-hydroxy-3,3-dimethylbutan-2-yl]carbamoyl}benzoic acid", "protease", "Homo sapiens", 2.2, "H" ], [ "4K78", "CFTR ASSOCIATED LIGAND (CAL) E317A PDZ DOMAIN BOUND TO PEPTIDE ICAL36-", "protein_interaction", "Homo sapiens", 1.8, "A" ], [ "4LMO", "STRUCTURE OF A VERTEBRATE RNA BINDING DOMAIN OF TELOMERASE (TRBD)", "polymerase", "TAKIFUGU RUBRIPES", 2.37, "B" ], [ "4LQI", "Ubiquitina-Proteasoma (4LQI)", "proteasome", "SACCHAROMYCES CEREVISIAE", 2.7, "K" ], [ "4MD6", "CRYSTAL STRUCTURE OF PDE5 IN COMPLEX WITH INHIBITOR 5R", "phosphodiesterase", "Homo sapiens", 2, "A" ], [ "4MS2", "STRUCTURAL BASIS OF CA2+ SELECTIVITY OF A VOLTAGE-GATED CALCIUM", "ion_channel", "ARCOBACTER BUTZLERI", 2.75, "A" ], [ "4NC3", "5-HT2B (HTR2B — Serotonin Receptor)", "gpcr", "Homo sapiens", 2.8, "A" ], [ "4NJT", "CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.95, "A" ], [ "4NJV", "CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.8, "A" ], [ "4NPU", "CRYSTAL STRUCTURE OF HIV-1 PROTEASE MULTIPLE MUTANT P51", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.5, "B" ], [ "4NY4", "CYP3A4 (Cytochrome P450)", "cytochrome_p450", "Homo sapiens", 2.95, "A" ], [ "4O1Z", "CRYSTAL STRUCTURE OF OVINE CYCLOOXYGENASE-1 COMPLEX WITH MELOXICAM", "oxidoreductase", "OVIS ARIES", 2.4, "A" ], [ "4OIV", "Structural basis for small molecule NDB as a selective antagonist of FXR", "nuclear_receptor", "Homo sapiens", 1.7, "A" ], [ "4PHL", "TBRPDEB1-INHIBITOR COMPLEX", "phosphodiesterase", "TRYPANOSOMA BRUCEI", 1.95, "A" ], [ "4PHU", "FFA1/GPR40 Free Fatty Acid", "gpcr", "Homo sapiens", 2.33, "A" ], [ "4PXZ", "Crystal structure of P2Y12 receptor in complex with 2MeSADP", "gpcr", "Homo sapiens", 2.5, "A" ], [ "4QA0", "CRYSTAL STRUCTURE OF C153F HDAC8 IN COMPLEX WITH SAHA", "hydrolase", "Homo sapiens", 2.24, "A" ], [ "4QGE", "PHOSPHODIESTERASE-9A IN COMPLEX WITH INHIBITOR WYQ-C36D", "phosphodiesterase", "PAN TROGLODYTES", 2, "A" ], [ "4RUR", "Ubiquitina-Proteasoma (4RUR)", "proteasome", "SACCHAROMYCES CEREVISIAE S288C", 2.5, "L" ], [ "4RVI", "CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.99, "A" ], [ "4RVJ", "CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.6, "A" ], [ "4W1V", "Crystal structure of 7,8-diaminopelargonic acid synthase (BioA) from Mycobacterium tuberculosis, complexed with a thiazole inhibitor", "transferase", "Mycobacterium tuberculosis", 2.24, "B" ], [ "4WUD", "N-TERMINAL 43 KDA FRAGMENT OF THE E. COLI DNA GYRASE B SUBUNIT GROWN", "topoisomerase", "ESCHERICHIA COLI STRAIN K-12", 1.95, "A" ], [ "4X8V", "FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (methyl {3-[(2R)-1-{(2R)-2-(3,4-dimethoxyphenyl)-2-[(1-oxo-1,2,3,4-tetrahydroisoquinolin-7-yl)amino]acetyl}pyrrolidin-2-yl]-4-(propan-2-ylsulfonyl)phenyl}carbamate)", "protease", "Homo sapiens", 2.5, "H" ], [ "4Y79", "Factor Xa Coagulation", "protease", "Homo sapiens", 2.1, "A" ], [ "4YNQ", "TREX1-dsDNA complex", "nuclease", "MUS MUSCULUS", 2.8, "H" ], [ "4YX9", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF BOUND TO", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 1.75, "A" ], [ "4ZUD", "Crystal Structure of Human Angiotensin Receptor in Complex with Inverse Agonist Olmesartan at 2.8A resolution.", "gpcr", "Homo sapiens", 2.8, "A" ], [ "4ZVI", "GYRASE B IN COMPLEX WITH 4,5-DIBROMOPYRROLAMIDE-BASED INHIBITOR", "topoisomerase", "ESCHERICHIA COLI", 2.2, "A" ], [ "4ZZZ", "Structure of human PARP1 catalytic domain bound to an isoindolinone inhibitor", "methyltransferase", "Homo sapiens", 1.9, "A" ], [ "5A2R", "A New Crystal Structure of the Drosophila melanogaster Angiotensin Converting Enzyme Homologue AnCE.", "protease", "DROSOPHILA MELANOGASTER", 1.85, "A" ], [ "5AXQ", "CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH", "phosphodiesterase", "Homo sapiens", 1.77, "A" ], [ "5C9H", "STRUCTURAL BASIS OF TEMPLATE BOUNDARY DEFINITION IN TETRAHYMENA", "polymerase", "TETRAHYMENA THERMOPHILA", 3, "E" ], [ "5CON", "X-RAY CRYSTAL STRUCTURE OF WILD TYPE HIV-1 PROTEASE IN COMPLEX WITH", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.8, "A" ], [ "5COP", "X-RAY CRYSTAL STRUCTURE OF WILD TYPE HIV-1 PROTEASE IN COMPLEX WITH", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 2, "A" ], [ "5CQG", "STRUCTURE OF TRIBOLIUM TELOMERASE IN COMPLEX WITH THE HIGHLY SPECIFIC", "polymerase", "TRIBOLIUM CASTANEUM", 2.3, "A" ], [ "5CZ6", "Ubiquitina-Proteasoma (5CZ6)", "proteasome", "SACCHAROMYCES CEREVISIAE (STRAIN ATCC 204508 /", 2.7, "H" ], [ "5CZ7", "Ubiquitina-Proteasoma (5CZ7)", "proteasome", "SACCHAROMYCES CEREVISIAE (STRAIN ATCC 204508 /", 2.5, "H" ], [ "5DIY", "THERMOBACULUM TERRENUM O-GLCNAC HYDROLASE MUTANT - D120N", "hydrolase", "Homo sapiens", 2.06, "A" ], [ "5E4G", "CRYSTAL STRUCTURE OF HUMAN GROWTH DIFFERENTIATION FACTOR 11 (GDF-11)", "growth_factor", "Homo sapiens", 1.5, "A" ], [ "5E8V", "TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A,", "kinase", "Homo sapiens", 1.69, "A" ], [ "5E8Y", "TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A,", "kinase", "Homo sapiens", 2.05, "A" ], [ "5E91", "TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A,", "kinase", "Homo sapiens", 2.42, "A" ], [ "5E92", "TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A,", "kinase", "Homo sapiens", 2.08, "A" ], [ "5EPN", "Crystal structure of HCV NS3/4A protease in complex with 5172-mcP1P3 (MK-5172 P1-P3 macrocyclic analogue)", "protease", "Hepatitis C virus", 2.3, "A" ], [ "5F1A", "THE CRYSTAL STRUCTURE OF SALICYLATE BOUND TO HUMAN CYCLOOXYGENASE-2", "oxidoreductase", "Homo sapiens", 2.38, "A" ], [ "5F4W", "Tagatose-1,6-bisphosphate aldolase from Streptococcus pyogenes in complex with TBP", "lyase", "Streptococcus pyogenes serotype M1", 1.66, "A" ], [ "5FG9", "Ubiquitina-Proteasoma Target (5FG9)", "proteasome", "SACCHAROMYCES CEREVISIAE S288C", 2.6, "P" ], [ "5FPW", "PROCATHEPSIN B S9 FROM TRYPANOSOMA CONGOLENSE", "protease", "TRYPANOSOMA CONGOLENSE", 2.1, "A" ], [ "5HK9", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF BOUND TO A UREA", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 1.8, "A" ], [ "5HKA", "CRYSTAL STRUCTURE OF THE CFTR INHIBITORY FACTOR CIF BOUND TO AN AMIDE", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 2.05, "A" ], [ "5HYK", "Crystal structure of the complex PPARalpha/AL26-29", "nuclear_receptor", "Homo sapiens", 1.83, "A" ], [ "5I3T", "Native Structure of the Linalool Dehydratase-Isomerase from Castellaniella defragrans", "isomerase", "Castellaniella defragrans", 2.1, "A" ], [ "5J89", "PD-L1 (CD274)", "protein_interaction", "Homo sapiens", 2.2, "C" ], [ "5JHW", "CRYSTAL STRUCTURE OF THE GDF11:FOLLISTATIN 288 COMPLEX", "growth_factor", "Homo sapiens", 2.35, "A" ], [ "5JYC", "CRYSTAL STRUCTURE OF THE E153Q MUTANT OF THE CFTR INHIBITORY FACTOR", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 2, "A" ], [ "5L2I", "The X-ray co-crystal structure of human CDK6 and Palbociclib.", "kinase", "Homo sapiens", 2.75, "A" ], [ "5L2Y", "Factor VIIa in complex with the inhibitor 1-[(2R,15R)-2-[(1-amino-4-fluoroisoquinolin-6-yl)amino]-4,15,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.1~6,10~]henicosa-1(18),6,8,10(21),16,19-hexaen-7-yl] cyclobutane-1-carboxylic acid", "protease", "Homo sapiens", 1.82, "H" ], [ "5L2Z", "Factor VIIa in complex with the inhibitor 1-[(2R,15R)-2-[(1-amino-4-fluoroisoquinolin-6-yl)amino]-4,15,17-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.1~6,10~]henicosa-1(18),6(21),7,9,16,19-hexaen-7-yl]cyclohexane-1-carboxylic acid", "protease", "Homo sapiens", 1.79, "H" ], [ "5L30", "Factor VIIa in complex with the inhibitor (2R,15R)-2-[(1-aminoisoquinolin-6-yl)amino]-4,15,17-trimethyl-7-[1-(1H-tetrazol-5-yl)cyclopropyl]-13-oxa-4,11-diazatricyclo[14.2.2.1~6,10~]henicosa-1(18),6(21),7,9,16,19-hexaene-3,12-dione", "protease", "Homo sapiens", 1.73, "H" ], [ "5L3J", "ESCHERICHIA COLI DNA GYRASE B IN COMPLEX WITH BENZOTHIAZOLE-BASED", "topoisomerase", "ESCHERICHIA COLI", 2.83, "A" ], [ "5LSH", "human lysozyme in complex with a tetrasaccharide fragment of the O-chain of LPS from Klebsiella pneumoniae", "hydrolase", "Homo sapiens", 1.06, "A" ], [ "5ML2", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX WITH INHIBITOR-3", "phosphodiesterase", "Homo sapiens", 1.6, "B" ], [ "5ML3", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX TO DELTASONAMIDE1", "phosphodiesterase", "Homo sapiens", 1.4, "B" ], [ "5ML4", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX TO INHIBITOR-7", "phosphodiesterase", "Homo sapiens", 2.4, "B" ], [ "5ML6", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX TO INHIBITOR-8", "phosphodiesterase", "Homo sapiens", 1.87, "B" ], [ "5ML8", "THE CRYSTAL STRUCTURE OF PDE6D IN COMPLEX TO INHIBITOR-4", "phosphodiesterase", "Homo sapiens", 2.6, "B" ], [ "5MMN", "E. COLI DNA GYRASE B 24 KDA ATPASE DOMAIN IN COMPLEX WITH 1-ETHYL-3-", "topoisomerase", "ESCHERICHIA COLI O157:H7", 1.9, "A" ], [ "5NDD", "Crystal structure of a thermostabilised human protease-activated receptor-2 (PAR2) in complex with AZ8838 at 2.8 angstrom resolution", "gpcr", "Homo sapiens", 2.8, "A" ], [ "5NN5", "Crystal structure of human lysosomal acid-alpha-glucosidase, GAA, in complex with 1-deoxynojirimycin", "hydrolase", "Homo sapiens", 2, "A" ], [ "5NPT", "STRUCTURE OF THE N-TERMINAL DOMAIN OF THE YEAST TELOMERASE REVERSE", "polymerase", "OGATAEA POLYMORPHA", 2.4, "A" ], [ "5O65", "CRYSTAL STRUCTURE OF THE PSEUDOMONAS FUNCTIONAL AMYLOID SECRETION", "protein_interaction", "PSEUDOMONAS SP. UK4", 2.5, "A" ], [ "5O67", "CRYSTAL STRUCTURE OF THE FAPF POLYPEPTIDE TRANSPORTER - F103A MUTANT", "transporter", "PSEUDOMONAS SP. UK4", 2.84, "C" ], [ "5PA9", "Crystal Structure of Factor VIIa in complex with phenylmethanamine;hydrochloride", "protease", "Homo sapiens", 1.55, "C" ], [ "5QTS", "PanDDA analysis group deposition -- Crystal Structure of NUDT5 in complex with 8J-537S", "hydrolase", "Homo sapiens", 1.85, "B" ], [ "5RFY", "PanDDA analysis group deposition -- Crystal Structure of SARS-CoV-2 main protease in complex with PCM-0102974", "protease", "Severe acute respiratory syndrome coronavirus 2", 1.9, "A" ], [ "5TBO", "Crystal structure of Plasmodium falciparum dihydroorotate dehydrogenase bound with Inhibitor DSM421", "oxidoreductase", "Plasmodium falciparum (isolate 3D7)", 2.15, "A" ], [ "5TFT", "CYP2D6", "cytochrome_p450", "Homo sapiens", 2.71, "A" ], [ "5TGZ", "CB1 Cannabinoid Receptor", "gpcr", "Homo sapiens", 2.8, "A" ], [ "5TNE", "CRYSTAL STRUCTURE OF THE E153Q MUTANT OF THE CFTR INHIBITORY FACTOR", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 1.75, "A" ], [ "5TNH", "CRYSTAL STRUCTURE OF THE E153Q MUTANT OF THE CFTR INHIBITORY FACTOR", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 2.1, "C" ], [ "5TNN", "CRYSTAL STRUCTURE OF THE E153Q MUTANT OF THE CFTR INHIBITORY FACTOR", "ion_channel", "PSEUDOMONAS AERUGINOSA (STRAIN UCBPP-PA14)", 1.95, "A" ], [ "5TOL", "CRYSTAL STRUCTURE OF BETA-SITE APP-CLEAVING ENZYME 1 COMPLEXED WITH N-", "protease", "Homo sapiens", 2.51, "A" ], [ "5TPT", "THE CRYSTAL STRUCTURE OF AMYLOID PRECURSOR-LIKE PROTEIN 2 (APLP2) E2", "protein_interaction", "Homo sapiens", 2.42, "A" ], [ "5TUN", "CRYSTAL STRUCTURE OF UNINHIBITED HUMAN CATHEPSIN K AT 1.62 ANGSTROM", "protease", "Homo sapiens", 1.62, "A" ], [ "5TY1", "Identification of a New Zinc Binding Chemotype by Fragment Screening", "metalloenzyme", "Homo sapiens", 1.6, "A" ], [ "5U6X", "COX-1:P6 COMPLEX STRUCTURE", "oxidoreductase", "OVIS ARIES", 2.93, "A" ], [ "5VA1", "hERG (KCNH2 — Potassium Channel)", "ion_channel", "Homo sapiens", 3.7, "A" ], [ "5WBE", "COX-1:MOFEZOLAC COMPLEX STRUCTURE", "oxidoreductase", "OVIS ARIES", 2.75, "A" ], [ "5WIU", "Structure of the human D4 Dopamine receptor in complex with Nemonapride", "gpcr", "Homo sapiens", 1.96, "A" ], [ "5WZX", "Structural basis for a pentacyclic oleanane-type triterpenoid as a ligand of FXR", "nuclear_receptor", "Homo sapiens", 2.95, "A" ], [ "5YUA", "CRYSTAL STRUCTURE OF VOLTAGE-GATED SODIUM CHANNEL NAVAB IN HIGH-PH", "ion_channel", "ARCOBACTER BUTZLERI", 2.8, "A" ], [ "5YWS", "Crystal structure of TREX1 in complex with a Y structured DNA", "nuclease", "MUS MUSCULUS", 2, "A" ], [ "5YWV", "Crystal structure of TREX1 in complex with a inosine contained ssDNA", "nuclease", "MUS MUSCULUS", 2.3, "A" ], [ "5Z2R", "ThDP-Mn2+ complex of R395K variant of EcMenD soaked with 2-ketoglutarate for 5 min", "transferase", "Escherichia coli (strain K12)", 2.3, "A" ], [ "5ZBH", "The Crystal Structure of Human Neuropeptide Y Y1 Receptor with BMS-193885", "gpcr", "Homo sapiens", 3, "A" ], [ "6A5W", "FXR-LBD WITH HNC143 AND SRC1", "kinase", "Homo sapiens", 2.88, "A" ], [ "6B3J", "6B3J", "gpcr", "Homo sapiens", 3.3, "R" ], [ "6BOS", "Human APE1 substrate complex with an A/C mismatch adjacent the THF", "nuclease", "Homo sapiens", 2.3, "A" ], [ "6C1P", "HypoPP mutant", "ion_channel", "ARCOBACTER BUTZLERI (STRAIN RM4018)", 2.9, "A" ], [ "6CM4", "Structure of the D2 Dopamine Receptor Bound to the Atypical Antipsychotic Drug Risperidone", "gpcr", "Homo sapiens", 2.87, "A" ], [ "6E53", "STRUCTURE OF TERT IN COMPLEX WITH A NOVEL TELOMERASE INHIBITOR", "polymerase", "TRIBOLIUM CASTANEUM", 2.8, "A" ], [ "6EU9", "CRYSTAL STRUCTURE OF PLATYNEREIS DUMERILII RAR LIGAND-BINDING DOMAIN", "nuclear_receptor", "PLATYNEREIS DUMERILII", 2.69, "B" ], [ "6FBQ", "Crystal Structure of the Human Retinoid X Receptor DNA-Binding Domain Bound to the Human MEp DR1 Response Element, pH 7.0", "nuclear_receptor", "Homo sapiens", 1.6, "A" ], [ "6G2O", "X-ray structure of NSD3-PWWP1 in complex with compound BI-9321", "protein_interaction", "Homo sapiens", 1.81, "A" ], [ "6GAV", "EXTREMELY 'OPEN' CLAMP STRUCTURE OF DNA GYRASE: ROLE OF THE", "topoisomerase", "MYCOBACTERIUM TUBERCULOSIS", 2.6, "A" ], [ "6GUE", "CDK2/CyclinA in complex with AZD5438", "kinase", "Homo sapiens", 1.99, "A" ], [ "6HL0", "CRYSTAL STRUCTURE OF FARNESOID X RECEPTOR (FXR) WITH BOUND NCOA-2", "nuclear_receptor", "Homo sapiens", 1.66, "A" ], [ "6HL1", "FXR Bile Acid Receptor", "nuclear_receptor", "Homo sapiens", 1.6, "A" ], [ "6HSK", "CRYSTAL STRUCTURE OF A HUMAN HDAC8 L6 LOOP MUTANT COMPLEXED WITH", "hydrolase", "Homo sapiens", 2.1, "A" ], [ "6HW5", "Ubiquitina-Proteasoma (6HW5)", "proteasome", "SACCHAROMYCES CEREVISIAE (STRAIN ATCC 204508 /", 2.9, "H" ], [ "6HW7", "Ubiquitina-Proteasoma (6HW7)", "proteasome", "SACCHAROMYCES CEREVISIAE S288C", 2.7, "H" ], [ "6ITM", "CRYSTAL STRUCTURE OF FXR IN COMPLEX WITH AGONIST XJ034", "nuclear_receptor", "Homo sapiens", 2.5, "A" ], [ "6KE5", "STRUCTURE OF CAVAB IN COMPLEX WITH DILTIAZEM AND AMLODIPINE", "ion_channel", "ARCOBACTER BUTZLERI RM4018", 2.8, "C" ], [ "6LU7", "SARS-CoV-2 Mpro", "protease", "Severe acute respiratory syndrome coronavirus 2", 2.16, "A" ], [ "6MEO", "Structural basis of coreceptor recognition by HIV-1 envelope spike", "protein_interaction", "Homo sapiens", 3.9, "G" ], [ "6MK9", "X-RAY CRYSTAL STRUCTURE OF DARUNAVIR-RESISTANT-P51 HIV-1 PROTEASE IN", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.7, "A" ], [ "6MKL", "X-RAY CRYSTAL STRUCTURE OF DARUNAVIR-RESISTANT-P51 HIV-1 PROTEASE IN", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.7, "A" ], [ "6MVV", "NAVAB VOLTAGE-GATED SODIUM CHANNEL, I217C/F203A", "ion_channel", "ARCOBACTER BUTZLERI (STRAIN RM4018)", 2.9, "C" ], [ "6MVW", "NavAb voltage-gated sodium channel, I217C/F203W", "ion_channel", "Arcobacter butzleri (strain RM4018)", 3.2, "A" ], [ "6MWA", "NAVAB VOLTAGE-GATED SODIUM CHANNEL, RESIDUES 1-239", "ion_channel", "ARCOBACTER BUTZLERI (STRAIN RM4018)", 2.4, "B" ], [ "6N7B", "Structure of the human JAK1 kinase domain with compound 38", "kinase", "Homo sapiens", 1.81, "A" ], [ "6NTW", "Crystal structure of E. coli YcbB", "transferase", "Escherichia coli (strain K12)", 2.76, "A" ], [ "6OGV", "X-RAY CRYSTAL STRUCTURE OF DARUNAVIR-RESISTANT HIV-1 PROTEASE (P30) IN", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.57, "A" ], [ "6P3D", "The co-crystal structure of BRAF(V600E) with ponatinib", "kinase", "Homo sapiens", 2.11, "A" ], [ "6P6X", "CRYSTAL STRUCTURE OF VOLTAGE-GATED SODIUM CHANNEL NAVAB G94C/Q150C", "ion_channel", "ARCOBACTER BUTZLERI (STRAIN RM4018)", 2.75, "A" ], [ "6PS2", "beta-2 Adrenergic Receptor", "gpcr", "Homo sapiens", 2.4, "A" ], [ "6PU8", "ROOM TEMPERATURE X-RAY STRUCTURE OF HIV-1 PROTEASE TRIPLE MUTANT", "protease", "HUMAN IMMUNODEFICIENCY VIRUS 1", 1.8, "A" ], [ "6RML", "Crystal structure of TOPBP1 BRCT0,1,2 in complex with a 53BP1 phosphopeptide", "protein_interaction", "Homo sapiens", 2.81, "A" ], [ "6S1Y", "CRYSTAL STRUCTURE OF ANOPHELES GAMBIAE ANOACE2 IN COMPLEX WITH GAMMA-", "protease", "ANOPHELES GAMBIAE", 2.2, "A" ], [ "6S1Z", "CRYSTAL STRUCTURE OF ANOPHELES GAMBIAE ANOACE2 IN COMPLEX WITH", "protease", "ANOPHELES GAMBIAE", 2.5, "A" ], [ "6SX5", "FULL LENGTH MUTANT OPEN-FORM SODIUM CHANNEL NAVMS", "ion_channel", "MAGNETOCOCCUS MARINUS (STRAIN ATCC BAA-1437 /", 2.2, "A" ], [ "6SX7", "CRYSTAL STRUCTURE OF THE VOLTAGE-GATED SODIUM CHANNEL NAVMS (F208L)", "ion_channel", "MAGNETOCOCCUS MARINUS MC-1", 2.5, "A" ], [ "6SXC", "CRYSTAL STRUCTURE OF THE VOLTAGE-GATED SODIUM CHANNEL NAVMS (F208L) IN", "ion_channel", "MAGNETOCOCCUS MARINUS MC-1", 2.5, "A" ], [ "6SXE", "CRYSTAL STRUCTURE OF THE VOLTAGE-GATED SODIUM CHANNEL NAVMS (F208L) IN", "ion_channel", "MAGNETOCOCCUS MARINUS MC-1", 2.6, "A" ], [ "6SXG", "CRYSTAL STRUCTURE OF THE VOLTAGE-GATED SODIUM CHANNEL NAVMS IN COMPLEX", "ion_channel", "MAGNETOCOCCUS MARINUS MC-1", 2.4, "A" ], [ "6U26", "PCSK9 Allosteric", "protease", "Homo sapiens", 1.53, "B" ], [ "6USO", "TELOMERASE REVERSE TRANSCRIPTASE PRENUCLEOTIDE BINARY COMPLEX,", "polymerase", "TRIBOLIUM CASTANEUM", 2.54, "A" ], [ "6USR", "TELOMERASE REVERSE TRANSCRIPTASE TERNARY COMPLEX, TERT:DNA:DGPCPP", "polymerase", "TRIBOLIUM CASTANEUM", 2.93, "A" ], [ "6W10", "Structure of mouse TREX1 with E198K disease-associated mutation", "nuclease", "MUS MUSCULUS", 1.8, "B" ], [ "6WHA", "HTR2A bound to 25-CN-NBOH in complex with a mini-Galpha-q protein, beta/gamma subunits and an active-state stabilizing single-chain variable fragment (scFv16) obtained by cryo-electron microscopy (cryoEM)", "gpcr", "Homo sapiens", 3.36, "A" ], [ "6X1A", "GLP-1R (TMD / Oral Agonist Pocket)", "gpcr", "Homo sapiens", 2.5, "R" ], [ "6Y5A", "SEROTONIN-BOUND 5-HT3A RECEPTOR IN SALIPRO", "gpcr", "MUS MUSCULUS", 2.8, "A" ], [ "6Y5E", "Structure of human cGAS (K394E) bound to the nucleosome (focused refinement of cGAS-NCP subcomplex)", "transferase", "Homo sapiens", 3.15, "J" ], [ "6ZD1", "STRUCTURE OF APO TELOMERASE FROM CANDIDA TROPICALIS", "polymerase", "CANDIDA TROPICALIS MYA-3404", 2.47, "A" ], [ "6ZD2", "STRUCTURE OF APO TELOMERASE FROM CANDIDA TROPICALIS TRUNCATED FROM C-", "polymerase", "CANDIDA TROPICALIS MYA-3404", 2.84, "A" ], [ "6ZD6", "STRUCTURE OF APO TELOMERASE FROM CANDIDA TROPICALIS", "polymerase", "CANDIDA TROPICALIS MYA-3404", 2.64, "A" ], [ "6ZDP", "STRUCTURE OF TELOMERASE FROM CANDIDA TROPICALIS IN COMPLEXE WITH TWJ", "polymerase", "CANDIDA TROPICALIS (STRAIN ATCC MYA-3404 / T1)", 2.85, "A" ], [ "6ZDQ", "STRUCTURE OF TELOMERASE FROM CANDIDA ALBICANS IN COMPLEXE WITH TWJ", "polymerase", "CANDIDA ALBICANS SC5314", 2.98, "C" ], [ "7BVQ", "Structure of human beta1 adrenergic receptor bound to carazolol", "gpcr", "Homo sapiens", 2.5, "A" ], [ "7D42", "Structural basis of tropifexor as a potent and selective agonist for farnesoid X receptor", "nuclear_receptor", "Homo sapiens", 2.7, "A" ], [ "7DFL", "H1 Histamine Receptor", "gpcr", "Homo sapiens", 3.3, "R" ], [ "7E2Y", "5-HT1A", "gpcr", null, 3, "R" ], [ "7JVU", "CRYSTAL STRUCTURE OF HUMAN HISTONE DEACETYLASE 8 (HDAC8) I45T MUTATION", "hydrolase", "Homo sapiens", 1.5, "A" ], [ "7JVW", "CRYSTAL STRUCTURE OF HUMAN HISTONE DEACETYLASE 8 (HDAC8) G320R", "hydrolase", "Homo sapiens", 2.4, "A" ], [ "7KQM", "BINARY COMPLEX OF TERT (TELOMERASE REVERSE TRANSCRIPTASE) WITH", "polymerase", "TRIBOLIUM CASTANEUM", 2.73, "A" ], [ "7PAC", "THE CRYSTAL STRUCTURE OF PDE6D IN THE APO STATE", "phosphodiesterase", "Homo sapiens", 2.05, "B" ], [ "7SBE", "STRUCTURE OF THE K. LACTIS TELOMERASE RNA BINDING DOMAIN", "polymerase", "KLUYVEROMYCES LACTIS", 2.65, "B" ], [ "7SGG", "CRYSTAL STRUCTURE OF DANIO RERIO HISTONE DEACETYLASE 10 IN COMPLEX", "hydrolase", "DANIO RERIO", 2.1, "A" ], [ "7T9I", "NATIVE HUMAN TSH BOUND TO HUMAN THYROTROPIN RECEPTOR IN COMPLEX WITH", "gpcr", "Homo sapiens", 2.9, "N" ], [ "7T9N", "M22 AGONIST AUTOANTIBODY BOUND TO HUMAN THYROTROPIN RECEPTOR IN", "gpcr", "Homo sapiens", 2.9, "R" ], [ "7TM9", "CRYSTAL STRUCTURE OF BACTERIAL ALKALINE PHOSPHATASE FROM KLEBSIELLA", "hydrolase", "KLEBSIELLA PNEUMONIAE SUBSP. PNEUMONIAE", 1.95, "A" ], [ "7TRB", "CRYSTAL STRUCTURE OF FARNESOID X-ACTIVATED RECEPTOR COMPLEXED WITH", "nuclear_receptor", "Homo sapiens", 2.15, "A" ], [ "7UTZ", "HUMAN THYROTROPIN ANALOG TR1402 BOUND TO HUMAN THYROTROPIN RECEPTOR IN", "gpcr", "Homo sapiens", 2.4, "R" ], [ "7VUE", "Structural insight of the molecular mechanism of cilofexor bound to FXR", "nuclear_receptor", "Homo sapiens", 2.6, "A" ], [ "7XW5", "TSHR-THYROID STIMULATING HORMONE-GS-ML109 COMPLEX", "gpcr", "Homo sapiens", 2.96, "R" ], [ "7XW6", "TSHR-GS-M22 ANTIBODY-ML109 COMPLEX", "gpcr", "Homo sapiens", 2.78, "A" ], [ "7ZYJ", "Ubiquitina-Proteasoma (7ZYJ)", "proteasome", "LEISHMANIA TARENTOLAE", 2.7, "L" ], [ "8F6U", "CRYSTAL STRUCTURE OF NANOBODY VHH113 BOUND TO ITS ANTIGEN PA14 CIF", "protein_interaction", "PSEUDOMONAS AERUGINOSA PA14", 1.7, "C" ], [ "8F6V", "CRYSTAL STRUCTURE OF NANOBODY VHH108 BOUND TO ITS ANTIGEN PA14 CIF", "protein_interaction", "VICUGNA PACOS", 2.3, "B" ], [ "8GJR", "CRYSTAL STRUCTURE OF NANOBODY VHH114 BOUND TO ITS ANTIGEN PA14 CIF", "protein_interaction", "PSEUDOMONAS AERUGINOSA PA14", 1.85, "C" ], [ "8HCE", "Crystal structure of mTREX1-CMP complex", "nuclease", "MUS MUSCULUS", 1.5, "B" ], [ "8HCF", "Crystal structure of mTREX1-UMP complex", "nuclease", "MUS MUSCULUS", 1.6, "B" ], [ "8HD3", "FARNESOID X RECEPTOR AGONISTS_FXR FUSED WITH A HD3 PEPTIDE", "nuclear_receptor", "Homo sapiens", 2.29, "A" ], [ "8HFE", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN AN", "transporter", "Homo sapiens", 2.5, "A" ], [ "8HFF", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN THE", "transporter", "Homo sapiens", 2.86, "A" ], [ "8HFG", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN THE", "transporter", "Homo sapiens", 3, "A" ], [ "8HFI", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN THE", "transporter", "Homo sapiens", 2.5, "A" ], [ "8HFL", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN THE", "transporter", "Homo sapiens", 3, "A" ], [ "8I3V", "CRYO-EM STRUCTURE OF HUMAN NOREPINEPHRINE TRANSPORTER NET IN THE", "transporter", "Homo sapiens", 2.85, "A" ], [ "8J47", "CRYOEM STRUCTURE OF 40-RESIDUE ARCTIC (E22G) BETA-AMYLOID FIBRIL", "protein_interaction", "Homo sapiens", 2.5, "A" ], [ "8JSW", "HUMAN VMAT2 COMPLEX WITH SEROTONIN", "transporter", "Homo sapiens", 2.84, "A" ], [ "8JT9", "HUMAN VMAT2 COMPLEX WITH KETANSERIN", "transporter", "Homo sapiens", 2.97, "A" ], [ "8JTB", "VMAT2 COMPLEX WITH DOPAMINE", "transporter", "Homo sapiens", 2.93, "A" ], [ "8T69", "HUMAN VMAT2 IN COMPLEX WITH TETRABENAZINE", "transporter", "Homo sapiens", 2.89, "A" ], [ "8UBR", "COMPLEX OF THE PHOSPHORYLATED HUMAN CYSTIC FIBROSIS TRANSMEMBRANE", "ion_channel", "Homo sapiens", 2.7, "A" ], [ "8V52", "CRYSTAL STRUCTURE OF 2A10 FAB BOUND TO HUMAN TGF-BETA3", "growth_factor", "Homo sapiens", 2.5, "F" ], [ "8WGR", "CRYO-EM STRUCTURE OF INWARD-OPEN STATE HUMAN NOREPINEPHRINE", "transporter", "Homo sapiens", 2.75, "A" ], [ "8WRE", "HUMAN VMAT2 IN COMPLEX WITH DOPAMINE", "transporter", "Homo sapiens", 2.9, "A" ], [ "8WTW", "CRYO-EM STRUCTURE OF NORADRENALINE TRANSPORTER IN COMPLEX WITH A X-", "transporter", "Homo sapiens", 2.8, "A" ], [ "8WTX", "CRYO-EM STRUCTURE OF NORADRENALINE TRANSPORTER IN COMPLEX WITH", "transporter", "Homo sapiens", 2.9, "A" ], [ "8WZL", "ARABIDOPSIS THALIANA HISTONE DEACETYLASE 7 (HDA7)", "hydrolase", "ARABIDOPSIS THALIANA", 1.5, "A" ], [ "8X3K", "CRYO-EM STRUCTURE OF HUMAN VMAT2 IN COMPLEX WITH SEROTONIN", "transporter", "ESCHERICHIA COLI, HOMO SAPIENS", 2.98, "A" ], [ "8Y93", "STRUCTURE OF NET-AMITRIPTYLINE IN OUTWARD-OPEN STATE", "transporter", "Homo sapiens", 3, "A" ], [ "9E9G", "Heligmosomoides polygyrus TGF-beta Mimic 6 Domain 3 (TGM6-D3) Bound to Human TGF-beta Type II Receptor Extracellular Domain", "protein_interaction", "Homo sapiens", 1.4, "B" ], [ "9F9T", "Ubiquitina-Proteasoma Target (9F9T)", "proteasome", "TRYPANOSOMA CRUZI", 2.31, "M" ], [ "9GKV", "CRYSTAL STRUCTURE OF DEACETYLASE (HDAH) FROM VIBRIO CHOLERAE IN", "hydrolase", "VIBRIO CHOLERAE", 1.9, "B" ], [ "9KJE", "The apo-mTREX1 crystal structure for soaking experiments (Soaking Condition 2)", "nuclease", "MUS MUSCULUS", 1.4, "A" ], [ "9KQE", "CRYO-EM STRUCTURE OF HUMAN VMAT2 IN COMPLEX WITH DOPAMINE", "transporter", "ESCHERICHIA COLI, HOMO SAPIENS", 3, "A" ], [ "9NX5", "CRYSTAL STRUCTURE OF A P. AERUGINOSA GYRASE", "topoisomerase", "PSEUDOMONAS AERUGINOSA", 2.4, "A" ], [ "9QA0", "DROSOPHILA MELANOGASTER ANGIOTENSIN CONVERTING ENZYME HOMOLOGUE, ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.2, "A" ], [ "9QA1", "DROSOPHILA MELANOGASTER ANGIOTENSIN CONVERTING ENZYME HOMOLOGUE, ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.2, "A" ], [ "9QA2", "DROSOPHILA MELANOGASTER ANGIOTENSIN CONVERTING ENZYME HOMOLOGUE, ANCE", "protease", "BOS TAURUS", 1.9, "A" ], [ "9QA3", "DROSOPHILA MELANOGASTER ANGIOTENSIN CONVERTING ENZYME HOMOLOGUE, ANCE", "protease", "DROSOPHILA MELANOGASTER", 2.2, "A" ], [ "9QA4", "DROSOPHILA MELANOGASTER ANGIOTENSIN CONVERTING ENZYME HOMOLOGUE, ANCE", "protease", "BOS TAURUS", 1.85, "A" ], [ "9RAW", "THE L1 AMYLOID-BETA(1-40)FIBRIL IN THE PRESENCE OF ANLE138B (POST-", "protein_interaction", "Homo sapiens", 2.79, "A" ], [ "9RAX", "THE L1 AMYLOID-BETA(1-40)FIBRIL IN THE PRESENCE OF ANLE138B (PRE-", "protein_interaction", "Homo sapiens", 2.76, "A" ], [ "9RJE", "X-RAY STRUCTURE OF CHLAMYDOMONAS REINHARDTII HISTONE DEACETYLASE 11", "hydrolase", "CHLAMYDOMONAS REINHARDTII", 1.06, "A" ], [ "9TDZ", "Crystal structure of beta-TrCP bound by diphosphorylated claspin degron peptide", "ubiquitin_ligase", "Homo sapiens", 1.35, "A" ], [ "9V39", "CRYSTAL STRUCTURE OF DE NOVO DESIGNED SEROTONIN BINDER SROB2_30", "gpcr", "ESCHERICHIA COLI BL21(DE3)", 2.58, "A" ], [ "9V3A", "CRYSTAL STRUCTURE OF DE NOVO DESIGNED SEROTONIN BINDER SROB2_26_L7F", "gpcr", "ESCHERICHIA COLI BL21(DE3)", 2, "A" ], [ "7SRQ", "5-HT2B (HTR2B), LSD-bound cryo-EM receptor", "gpcr", "Homo sapiens", 2.7, "R" ] ], "unavailable": { "1EPB": "receptor_site_residues_missing", "1FEM": "mk_prepare_receptor", "1M9Z": "receptor_site_residues_missing", "1UZJ": "mk_prepare_receptor", "1VKG": "mk_prepare_receptor", "1XWD": "mk_prepare_receptor", "3HH2": "mk_prepare_receptor", "5I3T": "mk_prepare_receptor", "5NPT": "receptor_site_residues_missing", "6BOS": "receptor_site_residues_missing", "6NTW": "mk_prepare_receptor", "7D42": "mk_prepare_receptor", "8WTW": "mk_prepare_receptor" }, "warnings": { "1UZJ": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "1W22": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "2B2A": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "3KD2": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "3KDA": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "3V94": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4DLN": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4DM7": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4DMF": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4I04": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4LMO": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "4YNQ": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "5DIY": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "5YWV": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "7JVU": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ], "7JVW": [ "SITIO_FUERA_DE_LA_UNIDAD_BIOLOGICA" ] } }